Canonical Allele Identifier: CA2630737834

Gene: HBA2

Linked Data

• gnomAD v4: 16-173446-C-CCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173447_173448insCAC , CM000678.2:g.173447_173448insCAC	GRCh38
NC_000016.9:g.223446_223447insCAC , CM000678.1:g.223446_223447insCAC	GRCh37
NC_000016.8:g.163446_163447insCAC	NCBI36
NG_000006.1:g.34310_34311insCAC
NG_059186.1:g.1797_1798insCAC
NG_059271.1:g.5601_5602insCAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000251595.11:c.301-25_301-24insCAC MANE Select	ENSP00000251595.6:n.301-25_301-24insCAC
ENST00000251595.10:c.301-25_301-24insCAC	ENSP00000251595.6:n.301-25_301-24insCAC
ENST00000397806.1:c.205-25_205-24insCAC	ENSP00000380908.1:n.205-25_205-24insCAC
ENST00000482565.1:n.437-25_437-24insCAC
ENST00000484216.1:n.387_388insCAC
NM_000517.4:c.301-25_301-24insCAC	NP_000508.1:n.301-25_301-24insCAC
NM_000517.6:c.301-25_301-24insCAC MANE Select	NP_000508.1:n.301-25_301-24insCAC